FDA Medical devices recall ·
See Luer Cap Set, MPC-130, set, administration, intravascular recall
- Recall number
- Z-1774-2026
- Date
- (initiated February 17, 2026)
- Company / brand
- Molded Products Inc
1812 Industrial Pkwy, Harlan, IA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 26900 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
See Luer Cap Set, MPC-130, set, administration, intravascular
Why was it recalled?
Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI +B144MPC1300/$$529105203895, Lot Number 20389
Distribution
US Nationwide distribution in the states of TN, TX, NV, IL, FL.
States: Florida Illinois Nevada Tennessee Texas
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1774-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.